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. 2018 Mar 28;92(8):e02117-17.
doi: 10.1128/JVI.02117-17. Print 2018 Apr 15.

Shigella Phages Isolated during a Dysentery Outbreak Reveal Uncommon Structures and Broad Species Diversity

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Shigella Phages Isolated during a Dysentery Outbreak Reveal Uncommon Structures and Broad Species Diversity

Sarah M Doore et al. J Virol. .

Abstract

In 2016, Michigan experienced the largest outbreak of shigellosis, a type of bacillary dysentery caused by Shigella spp., since 1988. Following this outbreak, we isolated 16 novel Shigella-infecting bacteriophages (viruses that infect bacteria) from environmental water sources. Most well-known bacteriophages infect the common laboratory species Escherichia coli and Salmonella enterica, and these phages have built the foundation of molecular and bacteriophage biology. Until now, comparatively few bacteriophages were known to infect Shigella spp., which are close relatives of E. coli We present a comprehensive analysis of these phages' host ranges, genomes, and structures, revealing genome sizes and capsid properties that are shared by very few previously described phages. After sequencing, a majority of the Shigella phages were found to have genomes of an uncommon size, shared by only 2% of all reported phage genomes. To investigate the structural implications of this unusual genome size, we used cryo-electron microscopy to resolve their capsid structures. We determined that these bacteriophage capsids have similarly uncommon geometry. Only two other viruses with this capsid structure have been described. Since most well-known bacteriophages infect Escherichia or Salmonella, our understanding of bacteriophages has been limited to a subset of well-described systems. Continuing to isolate phages using nontraditional strains of bacteria can fill gaps that currently exist in bacteriophage biology. In addition, the prevalence of Shigella phages during a shigellosis outbreak may suggest a potential impact of human health epidemics on local microbial communities.IMPORTANCEShigella spp. bacteria are causative agents of dysentery and affect more than 164 million people worldwide every year. Despite the need to combat antibiotic-resistant Shigella strains, relatively few Shigella-infecting bacteriophages have been described. By specifically looking for Shigella-infecting phages, this work has identified new isolates that (i) may be useful to combat Shigella infections and (ii) fill gaps in our knowledge of bacteriophage biology. The rare qualities of these new isolates emphasize the importance of isolating phages on "nontraditional" laboratory strains of bacteria to more fully understand both the basic biology and diversity of bacteriophages.

Keywords: bacteriophage; cryo-electron microscopy; environmental microbiology; genomics; structural biology.

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Figures

FIG 1
FIG 1
Genome maps of representative isolates. Simplified representations of the Shigella phage genomes, using representative isolates from the groups defined in Fig. 2, are shown. The ruler is in kilobase pairs.
FIG 2
FIG 2
Genomic and phylogenetic analysis of environmental isolates. (A) Dot plot of all phage genomes compared with each other, including reference genomes of related phages shown in red. Species are separated by blue (long) lines, with individual isolates separated by red (short) lines. (B) Bayesian inference phylogenetic tree of environmental isolates. The scale bar represents 0.4 nucleotide substitutions per site.
FIG 3
FIG 3
Morphology of all phage isolates. Representative micrographs as viewed by negative-stain TEM are shown. The scale bar is 50 nm. Colored bars below the micrographs correspond to phylogenetic groups.
FIG 4
FIG 4
Cryo-electron microscopy and three-dimensional image reconstruction of a T=9 Shigella phage. (A) Representative micrograph of vitrified Sf14 particles. The arrow indicates the tail fibers visible on a representative virion. (B) Cryo-EM reconstruction of the capsid at ∼15-Å resolution, colored according to radial distance. (C) Enlarged view of the region in panel B outlined by the white box, illustrating the two types of hexamers. The black arrow indicates the presence of a decoration protein in one type of hexamer.

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